Neutron reactor having a xe shield



2,8ll,487 Patented Oct. 29, 1957 NEUTRON REACTR HAVING A Xe135 SHELD Henry E. Stanton, Chicago, Ill., assigner to the United States of America as represented by the United States Atomic Energy Commission Application December 3, 1946, Serial No. 713,653

1 Claim. (Cl. 24M-193.2)

This invention relates to neutronic reactors, and more particularly to a novel method and means for shielding such reactors against the ow of neutrons therefrom.

A Vgeneral object of the invention is to provide a novel lightweight neutron shield Iaround a neutronic reactor.

Another object of the invention is -to continuously withdraw from a neutronic reactor a highly neutronabsorbent fission product formed therewithin and to dispose said product around the reactor, externally thereof, for the purpose of absorbing neutrons emanating therefrom.

Still ,another object of the invention is to provide a novel composite neutron shield consisting of an 'inner layer of neutron moderator `adapted to slow escaping neutrons to relatively low energy values, and an outer layer of Xe135 which has an extremely great capture cross section for the slowed neutrons emanating yfrom the inner layer.

ylu neutronic reactors a neutron ssionable isotope, such as U223, U235, or 94239, or mixtures thereof is subjected to fission by absorption of neutrons, and a self-sustaining chain reaction is established by the neutrons evolved by the fission. In general, `such reactors comprise bodies of compositions containing such ssionable material, for example, natural uranium, disposed in `a neutron slowing material which slows the neutrons to thermal energies. Such a slowing material is termed a neutron moderator. Carbon, beryllium, and D20 (heavy water) are typical moderators suitable for such use. Heat is evolved during the reaction and is removed by passage of a coolant through the reactor in heat exchange relationship therewith. Specific details of the theory and essential characteristics of such reactors are set forth in the co-pending application of Enrico Fermi and Leo Szila-rd, Serial No. 568,904,V filed December 19, 1944, now Patent No. 2,708,656.

The ratio of the fast neutrons produced in one generation by the fissions to the original number of fast neutrons producing the fission in a system of infinite size from which there can be no escape is called the multiplication constant and is denoted by the symbol k. In a system of finite size, the ratio of the number of neutrons in one generationto the number of neutrons in theV preceding generation is called the reproduction ra-tio of thesystem, and is a constant designated by the symbol r. Usually this constant is expressed without .regard to localized neutron absorbers such as control or limiting rods, which are no-t uniformly dispersed throughout the entire system. The neutron reproduction ratio r is an actual value for a finite system, and differs from k by a factor due to loss of neutrons .through leakage and through absorption by localized neutron absorbers. To maintain a chain reaction, r must be at least equal to one. As pointed out in the above-mentioned Permi-Szilard application, it is preferably maintained below about 1.01 during operation of the reactor.

`In order that a self-'sustaining neutronic chain reaction can be established and maintained, the losses of neutrons must be held to a value so low that at least one neutron is available tor a new fission, after losses have been deducted, per neutron consumed in production of ssion. In fission of U235 and similar isotopes, more neutrons are evolved per fission than are required to produce the fission.

'For example, about 2.3 neutrons are evolved per neutron consumed in ssion of U235, and about 2.8 neutrons are evolved per neutron consumed in fission of 94239. These evolved neutrons are used up in fission of further U235 or 94239 atoms, or are lost to the reaction. `If losses do not reduce the ratio of neutrons evolved to neutrons consumed and Ilost below one, the chain reaction will continue. Losses may be external, as when neutrons escape fromA the reactor, or internal. Internal losses are caused by absorption of neutrons by atoms which do not ssion when the neutron has been absorbed.

U238 present in natural uranium absorbs substantial quantities of neutrons to produce 94239. VThis Vloss may be substantially reduced by use of uranium aggregate-s. Thu-s, it has lbeen found that U238 absorbs neutrons toan appreciable degree at energies (resonance energies) greater than thermal energies due to its relativelyhigh capture cross section with respect -to that of U235 at such resonance energies. However, this type of absorption, known as resonance absorption, may be reduced Iby decreasing the amount of neutrons which passV into a uranium body until these neutrons havebeen slowed to thermal energy. This maybe done -by reducing the ratio of surface area per unit weight of uranium, i. e., by using natural uranium in the form of aggregates preferably having a minimum thickness of about 0.5 cm. Moreover, this loss may be rendered negligible by use of a concentrate of a iissionable isotope which contains greater than natural concentration of fissionable material.

Neutron moderators also absorb neutrons. Generally speaking, it is desirable to use as a moderator an element (or compound thereof) of low atomic weightV and .low neutron capture cross section. The ability to slow downneutrons may be expressed by what is known as the scattering cross section, whereas the ability to absorb or capture neutrons may be expressed as the capture cross section. The ratio of absorption cross section to scattering cross section of various materials are' approximately as follows:

ight water (H2O) 0.00478 Diphenyl 0.00453 Beryllium 0.00127 Graphite 0.000726 Heavy water (D20) 0.00017 missible. .Using carbon or Ydeuterium oxide as moderators l and natural uranium as the fissionable composition, only about 1.1 or 1.3, respectively, neutrons are obtained per neutron consumed due to neutron losses in the U238 and the moderator. Since the external neutron losses may be substantial, other internal neutron losses should be held sufficiently 10W to prevent these losses from rising so high as to prevent the reaction.

Other components of the reactor including the coolant, impurities in the uranium or other portions of the system, moderator, control or limiting rods, fission fragments, restraining barrier, etc. absorb neutrons in varying amounts depending upon their neutron capture crosssection.

The eect of these impurities or absorbers in a reactor' containing natural uranium as the fissionable component has beenv approximately evaluated for each element aS,

a danger coefficient. This coefficient is computed according to the formula Element Danger Element Danger Coefficient Coefficient 15 10 1. 0 0. 01 2 50 310 .2 0. 04 18 2, 150 870 0. 012 54. 2 L 0 0. 18 0.002 1. 6 0. O2 1 3 1. 6 sa .s o. 3o o. 3o 25 0. 26 2. 4 Vo. a 2. 4 31 17 0.8 1, 430 2. 1 435 0.37 6, 320

1. s i 6 35 0. 61 2. 7 1 18 2 1. 7 6. 3 70 2. 5 2. 5 a 0. 4 40 0. 57 0. 5 0. 4 0. 03 0.13 0. 0025 0. 4 1. 1

The exceedingly large thermal neutron capture crosssection of Xe135 suggests the possibility of its use as a light weight shield for a neutronic reactor. If this possibility can be realized, great economies in weight and cost can be effected in the shielding problem through the elimination of massiveconcrete, etc.

It is well known that the `thickness of a neutron absorbing material for agiven transmission (i. e. the ratio of the emerging neutron ux tothe rimpinging flux) varies inversely with the product of the density of the absorber and its danger coefcient. Consequently, if x represents the thickness of an absorber, p and K its density and danger coeicients respectively,

Element p, glee. K 'x1/xn As an example of the use of this table, a shield thickness of 0.0033 cm of Xe in the form of a gas at normal temperature and pressure will transmit thermal neutrons the same as 1.0 cm. of iron. In other words, the fraction of neutrons absorbed in 0.0033 cm. of Xe135 is the same as in a 1.0 em. thickness of iron.

For purposes of shielding, the total mass of material is important. If the total mass of an absorber is designated by M, it follows from (2) that for the same transmission. Substitution into this equation from the table gives the following table:

Element M2 As an example, if l0 tons of iron is required to shield a pile, the same shielding could be accomplished with six grams of Xe135. y

In view of the fact that Xe135 decays with a half life of 9.5 hours, it is necessary to replenish it at frequent intervals to supply losses from decay, and also losses due to destruction by capture of the escaping neutrons. Under certain circumstances, these losses may be supplied by the reactor itself. Between 3% and 5% of all fissions lead to the formation of Xe135, and it is possible to recover a substantial portion of this gas in certain types of reactors.

On the other hand, each fission produces approximately two neutrons, one of which must be used, on the average, to maintainthe chain reaction. The excess neutrons must either be absorbed in the interior of the reactor or eventually leak out of the reactor. In consequence, the Xe135 in the shield vcan only absorb less than 5% of the neutrons generated by the tissions in order to regenerate the shield at a sutlicient rate to maintain it.

An alternative procedure would be to generate Xe135 by the bombardment with neutrons of Xe134, a stable isotope with an abundance of about 10%, but this is economically vnot feasible at present.

l An operative structure hereinafter described comprises a homogeneous liquid pile so loaded with absorbers (as thorium) that the neutronimultiplication constant for the innite pile would not Vexceed about 1.03. The Xe135 generated'is taken 0E continuously by sweeping it out with the other gases, or other means, and subsequently led into the shield space. The whole assembly is preferably surrounded by lead or other suitable material to shield against fy and other radiations. The Xe135 shield surrounds the reflector which'adequately slows the fast neutrons generated'in the active portion.

The foregoing and other/objects and advantages of the invention will be readily apparent from a consideration of the following specification and the accompanying drawing which comprises a iow diagram illustrating the invention as'applied to a system wherein the reactive composition and the neutron absorber are in fluid form.

The reactor, diagrammatically illustrated in the drawing, comprises a suspension such as a solution or slurry of a'ssionable material in a liquid moderator. For example, a solution of uranylsulphate in Water is chain reacting where the solution fills a spherical reactor 12 inches indiameter and surrounded with an eicient neutron reflector and 'where the reactor contains at least 575-600.*grams of U235 asa uranium concentrate containingabout 15% U235 based upon the total uranium. Higher amounts of U235 for example 600-700 or more grams are required where the reector'contains a neutron absorber as 'in the. 'present instance. 'Moreoven other solutions such as solutions of uranyl uoride, uranyl nitrate, plutonyl sulphate (PuOzSO-t) may be used where the-iissionable isotope content of the plutonium or uranium 1s above abolut 5-15% of the uranium or equivalent composition. In addition, natural uranium compounds (uranyl uoride U02 or UaOa) may be dispersed or dissolved in heavy water (D20) to establish a chain reaction.

The shape of the reactor may be cylindrical as shown by the drawings or may be spherical or other form. A slender elongated cylinder is particularly advantageous where maximum leakage is desired in order to secure a maximum of neutrons for bombardment of the neutron absorbent or `target isotope or isotopes.

In the gure, a reactor tank or chamber 2 of low neutron absorbing material, for example stainless steel or aluminum, is provided. This tank is sufficiently thin (for example 1A, inch or less) to permit passage of neutrons therethrough without substantial absorption of neutrons. The tank contains a chain reacting liquid composition 4 such as above-mentioned.

The reactive composition is continuously circulated through a heat exchanger 6 by means of a pump 8 having its suction side connected to the tank 2. The discharge side of the pump is connected to the heat exchanger 6 through which the reactive composition is passed in heat exchange relationship with a coolant circulated through the heat exchanger by inlet and outlet pipes 10 and 12. The cooled composition is returned to the tank 2 through a return line 14.

The amount of reactive composition Within the tank 2, as well as the concentration of uranium-containing material in the composition, is controlled by a system including a reversible delivery pump 16 connected to the bottom of the tank 2 and to a reservoir 18 having an inlet 20 to accommodate the introduction of uraniumcontaining material into said reservoir 18. The reservoir 18 is connected to the tank 2 through a line 22 having a conventional three-way operating valve 24 connected to the discharge side of :a pump 26, the suction side of which is connected to a moderator reservoir 30 having an inlet 32 through which moderator may be conveyed to this reservoir.

The reactive composition 4 is continuously Withdrawn from the bottom of the tank 2 through an outlet line 34 lconnected to the suction side of a pump 36, the discharge side of which is connected to a conventional separator device 38 adapted to separate the moderator from the uranium-containing material. Such a separator may comprise an evaporator or settling tank `and the separated material may be conveyed from the device 38 by an outlet line 40 for recovery of 94 and ssion products formed as a result of the neutronic reaction where natural uranium or U235-U238 mixtures are used Within the tank 2. Separated moderator is conveyed from the separator device 38 through a line 42 including a pump 44, the discharge side of which is connected to a moderator purier 46 from which the purified heavy Water is conveyed to the before-mentioned reservoir 30. The purilication may be effected by various means such as by distillation.

It will be understood that the water within the tank 2 is continuously decomposed into D2 and O2 or H2 and O2, depending upon the type of water used, as `a result of the neutronic reaction; and these decomposition products, as well :as gaseous fission products of the reaction including Xe135, are swept from the tank 2, and the decomposition products are recombined. A gas pump or blower 4S is provided having its suction side connected to a helium reservoir 50, and its discharge side connected to the tank 2 above the level of the reactive composition therein. The helium passes through the tank 2 and is conveyed therefrom by an outlet line 52 connected to a conventional recombiner device 54 adapted to recombine the hydrogen isotope or isotopes and Oz into vaporized D20 or H2O which is conveyed to a condenser 56, the

condensed D20v or H2O being conveyed to the beforementioned purifier tank 46. Helium is conveyed from the condenser 56 by a line 57, preferably including a pump or blower 58, to a separator tank 60 for removal of gaseous fission products and thence to the helium reservoir Si).

An emergency dump line 62 is connected to the tank 2 and the reservoir 18, said line including a dump valve 64 adapted to be opened under emergency conditions to reduce the body of composition 4 within the tank 2 to a size smaller than that at which a chain reaction may be sustained,

It may be noted that the system, thus far disclosed, is,

purely illustrative and such systems are more fully described in co-pending application, Serial No. 613,356, tiled August 29, 1945, in the United States Patent Otce by Eugene P. Wigner, Leo A. Ohlinger, Gale J. Young and Harcourt C. kVernon and also in an application of Robert F. Cristy, Serial No. 623,363, filed October 19, 1945.

Surrounding the tankkZ is another tank or chamber 66 within which a production area or zone containing a uid composition 68 to be bombarded by neutrons emanating from the reactor 2. This tank also is constructed of a low neutron absorber such as aluminum or stainless steel or other material having a danger coeilicient below l0 and having a thickness, e. g., s inch or less, sulliciently low to prevent substantial neutron absorption by the tank 66. The composition 68 may be a slurry or solution of the neutron absorbent material, such as thorium, in a neutron moderator such as heavy water, said composition being admitted to the chamber 66 through an inlet line 70 including a conventional shut-ott valve '72, After the composition 68 has been bombarded for the desired length of time, it is conveyedfrom the chamber 66 by an outlet line 74 including a conventional drain valve 76 to a conventional separator device '78 adapted to separate the heavy water from the neutron absorbent material which has at this point been converted to a radioactive isotope by the capture of neutrons as above discussed. The radioactive material is conveyed from the separator '78 by a line 80, and the separated moderator is conveyed from the device '78 by a line 82 connected to the suction side of the before-mentioned pump 44 which thus urges the heavy water from the line 82 to the beforementioned purifier tank 46. lt will be understood that the presently illustrated system will be used when the same moderator is used in tanks 2 and 66 and that where ditlerent moderators are used dicrent purifiers may be required.

The bombarded composition 68 is preferably circulated through a heat exchanger 84 by a pump 86 having its suction side connected to the chamber 66, the cooled composition being returned to the chamber 66 through a return pipe or line 88.

The chambers 2 and 66 are disposed within an aluminum or steel tank or chamber containing a heavy water neutron reector 92 adapted to reflect escaping neutrons back into the chamber 66 and/or reactor 2. The heavy water 92 is conveyed to the tank 96 through an inlet line 94 having a conventional shut-off valve 96 and is conveyed from the tank by an outlet line 98 having a conventional drain valve 16d.

The gaseous fission products which are separated from the helium in the separator 69 are pumped through a line 102 into a shield tank 164 by a pump having its discharge side connected to said tank. These fission products are expelled from the tank through an outlet line 10? which is connected to an exhaust Stack (not shown).

It will be understood that in a system such as above described Xel)5 constitutes about 25%-33% of the gaseous iission products swept from the chamber 2. rlhus the shield chamber formed between the tanks 90 and 164 must be about four times as thick as above described to replace an equivalent thickness of iron.V In other 7 words, approximately 0.0132 cm. of gas within'theshield chamber 110 is equivalent to 1 cm. thicknessof iron.

It may be` noted that the reflector 92 and thev gaseous'.

readily absorbed by Xe135 within the chamber. 111|).y Thus very few neutrons escape from the tank. 104 andx theseare preferably absorbed by a relatively. thinshield 112.y

of lead around this chamber adaptedlto--absorb game and other biological radiations.

Thus, it will be understood thatiLhave-designed.a\novel lightweight neutron shield which4 is capable of-.etctively shielding operating` personnel from. neutrons. emanating` from a neutronic reactor. Preferably:y this lightweight Xe135 shield withinthe chamber. 1-10Yis provided, .assabove described by extracting this. isotope from: the. reactive composition undergoing av chain. reaction.. However, it.

will be readily understood thatzif desired1the. Xe.135 may be Vproduced by bombarding Xe134 with neutrons. and-the chamber 110 may be iilled with. substantially purezXe135, an arrangement which would greatly reduce the thickness of the shield within the chamber 110.

It will be understood thatthe above-described embodiment of the invention is merely by way of illustration and not limitation inasmuch as variousv and other forms of the invention will be readily apparentto. those skilled in the art without departing from thespiritofthe invention or the scope of the appended claim.

What is claimed is:

A system of the class described, comprising a neutronic reactor comprising a reactor tank containingA a substantially homogeneous composition of thermal neutron lissionable material and liquid neutron moderator, a neutron reflector comprising a tank containing heavy; water-sur."v

rounding said. reactor, a shield tanksurroundingsaidrea ector, a gamma rayV shield surrounding;` said shieldvl tank-,. and means for conveying gaseousissionproducts includingv Xel35 vfrom the reactor chamber to the shieldy tank including` ak heliurnreservoir,c a blower for blowing helium gas through said reactor chamber,.afrecombiner, a condenser, and a separator tank for separating helium from the gaseous vssion products.

References Cited'in theiile. of this patent UNITED STATES PATENTS;

2,708,656v Fermiet al; May 17;` 1955.

2,716,705 Zinn` Aug. 3'0, 1955 2,743,225' Ohlinger etal Apr. 24, 1956 FOREIGN PATENTS 861,390 France Oct. 28, 1940 233,011 Switzerland'- Oct. 2, 1944? OTHER REFERENCES Atom Movements, pub. by American Society for Metals, 1951, Cleveland, Ohio, p. 175.

Introduction to Nuclear Eng., by- Richard Stephensom,

McGraw-Hill Book Co., New York, 1954, pp. 270-274.

Smyth: Ai General Account of` the Development of Methodsv of Using, Atomic Energy for Military Purposes Under theAuspicesof. the U. S; Government 1940-1945; p. 108, August 1945, also pp. 85, 102, 103.

Business Week, Sept. 1, 1945, pp. 58-64.

Katcoi: MDDCv 293. Date of ManuscriptApril 1956; date declass. Sept. 11, 1946; 14pages.

Kelly et al.: PhysicalReview, 73, 1135-9 (1948).

Hackhs- Chemical Dictionary, revised by Julius Grant, 3rd ed., 1950, Blak-iston Co., Philadelphia, p. 916. 

